Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,564 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,564 in last 12 months

Showing 2336123380 of 53,342 recalls

DrugApril 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: INOFOAM Foaming E-2 Food Handling Wash with .6% PCMX Recalled by Inopak Ltd...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: INODERM Antiseptic Hand Soap (E-2) Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Instant Waterless Hand Sanitizer Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Sani-Guard-SF Waterless Foam Hand Sanitizer Recalled by Inopak Ltd Due to...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: ANTIBACTERIAL Foaming Hand Wash With Moisturizers labeled as Antibacterial...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: AQUACIL instant foaming hand sanitizer Recalled by Inopak Ltd Due to CGMP...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2019· Cook Inc.

Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...

The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 19, 2019· Alvogen, Inc

Recalled Item: FENTANYL Transdermal System Recalled by Alvogen, Inc Due to Product Mix-Up:...

The Issue: Product Mix-Up: Customer complaint that their carton labeled as Fentanyl...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 19, 2019· Pacifico National, Inc. dba AmEx Pharmacy

Recalled Item: BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This...

The Issue: Defective Delivery System: difficult to express

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2019· Philips Healthcare Informatics, Inc.

Recalled Item: IntelliSpace PACS 4.4 Recalled by Philips Healthcare Informatics, Inc. Due...

The Issue: Images may potentially become corrupt while using the system.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· AURIS HEALTH INC

Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...

The Issue: Reports of aspirating biopsy needle breakage

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing